Aqueous multi-stage copolymer compositions for use in leather topcoats
US-10100377-B2 · Oct 16, 2018 · US
US11518905B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11518905-B2 |
| Application number | US-202017639378-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 22, 2020 |
| Priority date | Nov 19, 2019 |
| Publication date | Dec 6, 2022 |
| Grant date | Dec 6, 2022 |
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An aqueous coating composition comprising an aqueous dispersion of polyurethane and a siloxane-based polyamide.
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The invention claimed is: 1. An aqueous coating composition comprising: from 20 to 60 wt % of an aqueous dispersion of polyurethane, and from 0.5 to 10 wt % of a siloxane-based polyamide comprising a block copolymer comprising siloxane and amide blocks. 2. The aqueous coating composition of claim 1 , wherein the siloxane-based polyamide has the following physical properties: i) weight average molecular weight (Mw) of: 50,000 to 200,000 Daltons; ii) melting point range of 70 to 120° C.; iii) melt viscosity of 5000 to 10,000 cps at 140° C.; and iv) particle size of 0.1 to 15 micron. 3. The aqueous coating composition of claim 1 , wherein the siloxane amide block copolymer is represented by Formula A: wherein: (1) DP is 1-700; (2) n is a 1-500; (3) X is a divalent, aliphatic hydrocarbon group having 1-30 carbons; (4) Y is: (a) a divalent hydrocarbon group having 1-40 carbons, wherein the hydrocarbon group may optionally and additionally be substituted by at least one member selected from the group consisting of (i) hydroxy; (ii) a C3-C8 cycloalkyl; (iii) 1-3 members selected independently from the group consisting of C1-C3 alkyls and phenyl optionally substituted by 1-3 members selected independently from the group consisting of C1-C3 alkyls; (iv) a C1-C3 hydroxy alkyl; and (v) a C1-C6 alkyl amino, and the hydrocarbon group may optionally and additionally contain at least one of (i) 1-3 amide linkages; (ii) a C5 or C6 cyclic, divalent, saturated hydrocarbon group; and (iii) a phenylene optionally substituted by 1-3 members selected independently from the group consisting of C1-C3 alkyls, or (b) R 20 T(R 21 )R 22 , where R 20 and R 22 are divalent C1-C10 hydrocarbon groups and R 21 is a monovalent or divalent C1-C10 hydrocarbon group, such groups being independent of one another, and T is C(R), where is selected from hydrogen, R′, R 2 , R 3 , R 4 , or a trivalent N, P or Al; and (5) Each of R 1 , R 2 , R 3 and R 4 is independently selected from the group consisting of methyl, ethyl, propyl, isopropyl, a siloxane chain, and phenyl, wherein the phenyl may optionally be substituted at 1-3 positions by substituents independently selected from the group consisting of methyl and ethyl. 4. The aqueous coating composition of claim 3 wherein DP is 50 to 200 and n is 2 to 50. 5. The aqueous coating composition of claim 3 where R 1 , R 2 , R 3 and R 4 are all methyl; and X and Y are independently selected from a C4-C18 aliphatic hydrocarbon group. 6. The aqueous coating composition of claim 1 wherein the polyurethane has a Mw of: 150,000 to 1,500,000 Daltons.
macromolecular (C09D7/41-C09D7/48 take precedence) · CPC title
Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced {(electrically insulating plastics, resins or waxes H01B3/30)}; Filling pastes · CPC title
Polyurethanes · CPC title
using polymeric products of isocyanates (or isothiocyanates) with compounds having active hydrogen · CPC title
containing polyamide, polyesteramide or polyimide sequences · CPC title
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